4.5 Review

Research Progress on Histone Deacetylases Regulating Programmed Cell Death in Atherosclerosis

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5-Heptadecylresorcinol Protects against Atherosclerosis in Apolipoprotein E-Deficient Mice by Modulating SIRT3 Signaling: The Possible Beneficial Effects of Whole Grain Consumption

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Programmed cell death in atherosclerosis and vascular calcification

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Summary: The concept of cell death has expanded to include various forms such as necroptosis, pyroptosis, autophagy, and ferroptosis, in addition to apoptosis and necrosis. These different modes of cell death play critical roles in all aspects of life and have diverse implications in diseases. Atherosclerosis (AS) and vascular calcification (VC) are major causes of high morbidity and mortality in cardiovascular disease. Despite advancements in understanding the signaling pathways associated with AS and VC, the exact molecular basis remains unknown. This article reviews the molecular mechanisms underlying cell death and its implications for AS and VC, which may lead to the development of promising therapeutic strategies.

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Ruscogenin Alleviates Myocardial Ischemia-Induced Ferroptosis through the Activation of BCAT1/BCAT2

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HDAC11 promotes both NLRP3/caspase-1/GSDMD and caspase-3/GSDME pathways causing pyroptosis via ERG in vascular endothelial cells

Feng Yao et al.

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Sirt6 inhibits vascular endothelial cell pyroptosis by regulation of the Lin28b/let-7 pathway in atherosclerosis

Feng Yao et al.

Summary: This study found that Sirt6 inhibits vascular endothelial cell pyroptosis in atherosclerosis (AS) by negatively regulating the Lin28b/let-7 pathway.

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Xiang Wei et al.

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Sirtuin 3 deficiency exacerbates diabetic cardiomyopathy via necroptosis enhancement and NLRP3 activation

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Yoshiro Naito et al.

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Targeting HDAC6 attenuates nicotine-induced macrophage pyroptosis via NF-κB/NLRP3 pathway

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Polydatin alleviates high-fat diet induced atherosclerosis in apolipoprotein E-deficient mice by autophagic restoration

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HDAC1-mediated deacetylation of HIF1α prevents atherosclerosis progression by promoting miR-224-3p-mediated inhibition of FOSL2

Hao Wang et al.

Summary: The study showed that miR-224-3p reduces endothelial cell apoptosis, inflammatory responses, and ROS levels by targeting FOSL2, while HIF1 alpha promotes endothelial cell apoptosis and ROS accumulation. HDAC1 inhibits HIF1 alpha expression through deacetylation, enhancing the inhibitory effect of miR-224-3p and reducing endothelial cell apoptosis and ROS accumulation.

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Oxidative Stress Triggers Defective Autophagy in Endothelial Cells: Role in Atherothrombosis Development

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Summary: Atherothrombosis, a complex artery disorder, is a major cause of morbidity and mortality worldwide. Imbalance between oxidative stress and antioxidant defenses triggers cellular events leading to vascular wall remodeling and thrombus formation. Emerging studies focus on clotting activation and defective autophagy as potential therapeutic targets for atherosclerotic disease.

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Necroptosis, pyroptosis and apoptosis: an intricate game of cell death

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Summary: Cell death is a fundamental physiological process in all living organisms, playing important roles in embryonic development, organ maintenance, aging, immune responses, and autoimmunity. Recent research has significantly increased our understanding of the mechanisms orchestrating different types of programmed cell death and how they affect the balance of cell fates. Various modalities of cell death, such as apoptosis, necroptosis, and pyroptosis, have been studied to highlight both common and unique pathways and their impact on the surrounding cells and the organism as a whole.

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Downregulation of microRNA-512-3p enhances the viability and suppresses the apoptosis of vascular endothelial cells, alleviates autophagy and endoplasmic reticulum stress as well as represses atherosclerotic lesions in atherosclerosis by adjusting spliced/unspliced ratio of X-box binding protein 1 (XBP-1S/XBP-1U)

Peipei Ge et al.

Summary: miR-512-3p regulates the survival and migration of ox-LDL-treated endothelial cells by modulating XBP-1, playing a role in preventing and alleviating atherosclerosis.

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Activation of CD137 signaling promotes macrophage apoptosis dependent on p38 MAPK pathway-mediated mitochondrial fission

Yu Xu et al.

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Advanced research on the regulated necrosis mechanism in myocardial ischemia-reperfusion injury

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MicroRNA-146a-3p/HDAC1/KLF5/IKBα signal axis modulates plaque formation of atherosclerosis mice

Huajin Liu et al.

Summary: The study investigated the role of miR-146a-3p and HDAC1 in plaque formation in AS mice, indicating increased miR-146a-3p and KLF5 levels, and decreased HDAC1 and IKB alpha levels in aortic wall tissues. Depletion of miR-146a-3p or restoration of HDAC1 led to improved stability of pathological plaques and reduced inflammatory factors in AS mice.

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Yahya Sohrabi et al.

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SIRT1-autophagy axis inhibits excess iron-induced ferroptosis of foam cells and subsequently increases IL-1B and IL-18

Guangming Su et al.

Summary: Ferroptosis is associated with atherosclerosis, and activation of SIRT1 can inhibit ferroptosis and IL-1(3 and IL-18 levels in foam cells, providing a novel therapeutic target for AS.

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Oxymatrine attenuates oxidized low-density lipoprotein-induced HUVEC injury by inhibiting NLRP3 inflammasome-mediated pyroptosis via the activation of the SIRT1/Nrf2 signaling pathway

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CircRNA RSF1 regulated ox-LDL induced vascular endothelial cells proliferation, apoptosis and inflammation through modulating miR-135b-5p/HDAC1 axis in atherosclerosis

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Low shear stress induced vascular endothelial cell pyroptosis by TET2/SDHB/ROS pathway

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Haojie Wang et al.

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